The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Fibronectin-dependent collagen I deposition modulates the cell response to fibronectin
Abstract
Communication between cells and the extracellular matrix (ECM) is critical for regulation of cell growth, survival, migration, and differentiation. Remodeling of the ECM can occur under normal physiological conditions, as a result of tissue injury, and in certain pathological conditions. ECM remodeling leads to alterations in ECM composition and organization that can alter many aspects of cell behavior, including cell migration. The cell migratory response varies depending on the type, amount, and organization of ECM molecules present, as well as the integrin and proteoglycan repertoire of the cells. We and others have shown that the deposition of several ECM molecules, including collagen types I and III, depends on the presence and stability of ECM fibronectin. Hence, the effect of fibronectin and fibronectin matrix on cell function may partially depend on its ability to direct the deposition of collagen in the ECM. In this study, we used collagen-binding fibronectin mutants and recombinant peptides that interfere with fibronectin-collagen binding to show that fibronectin-dependent collagen I deposition regulates the cell migratory response to fibronectin. These data show that the ability of fibronectin to organize other proteins in the ECM is an important aspect of fibronectin function and highlight the importance of understanding how interactions between ECM proteins influence cell behavior.
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Cites
Ignotz, R. A., & Massagué, J. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)35666-1 · Cited by 2,492
Mao, J. R., Taylor, G., Dean, W. B., Wagner, D. R., Afzal, V., Lotz, J. C., Rubin, E. M., & Bristow, J. (2002) · Nature Genetics · doi:10.1038/ng850 · Cited by 261 · cited 2×
“Mice lacking tenascin X have reduced collagen I content and lower density of type I collagen fibrils in skin, despite normal collagen synthesis (51).”
BackgroundZoppi, N., Gardella, R., De Paepe, A., Barlati, S., & Colombi, M. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m312609200 · Cited by 107
All Six Modules of the Gelatin-binding Domain of Fibronectin Are Required for Full Affinity
Katagiri, Y., Brew, S. A., & Ingham, K. C. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m212512200 · Cited by 50
Cited by
Mechanical forces regulate the interactions of fibronectin and collagen I in extracellular matrix
Kubow, K. E., Vukmirovic, R., Zhe, L., Klotzsch, E., Smith, M. L., Gourdon, D., Luna, S., & Vogel, V. (2015) · Nature Communications · doi:10.1038/ncomms9026 · Cited by 344
Fibronectin: Molecular Structure, Fibrillar Structure and Mechanochemical Signaling
Dalton, C. J., & Lemmon, C. A. (2021) · Cells · doi:10.3390/cells10092443 · Cited by 319
Faurobert, E., Rome, C., Lisowska, J., Manet-Dupé, S., Boulday, G., Malbouyres, M., Balland, M., Bouin, A.-P., Kéramidas, M., Bouvard, D., et al. (2013) · Journal of Cell Biology · doi:10.1083/jcb.201303044 · Cited by 114
Zoppi, N., Ritelli, M., & Colombi, M. (2012) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2012.06.004 · Cited by 21
Metadata
- Authors
- Sottile, J., Shi, F., Rublyevska, I., Chiang, H.-Y., Lust, J., & Chandler, J.
- Venue
- American Journal of Physiology-Cell Physiology
- Publisher
- American Physiological Society
- Published
- 2007-12
- Volume
- 293
- Issue
- 6
- Pages
- C1934-C1946
- ISSN
- 0363-6143 (ISSN-L)
- 1522-1563
- OpenAlex
- W1966498333
- Cited by
- 191
- References
- 4
- FWCI
- 2.88
- Type
- journal article
- Language
- en
- Open access
- closed
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- Sottile, J., Shi, F., Rublyevska, I., Chiang, H.-Y., Lust, J., & Chandler, J. (2007). Fibronectin-dependent collagen I deposition modulates the cell response to fibronectin. American Journal of Physiology-Cell Physiology. https://doi.org/10.1152/ajpcell.00130.2007
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